This session offers a U.S. Food and Drug Administration Investigator's insights from sponsor inspections that will help you to identify and prevent the problems that may arise for your data and/or application during the collection of tens to hundreds of thousands of documents during a single trial.

CEU: 1.00 ACRP

Speaker:

Lakecha Lewis, International Inspection Cadre, U.S. Food and Drug Administration

Watch a Sneak Peek into the Session Content: